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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5823Generated: October 26, 2026

Hydrochloric Acid → 2-(4-fluorophenyl)-3,4-dihydro-2H-1,4-benzothiazine

https://huagongshe.com/reaction/5823

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
ReactantSodium borohydrideHCID 4311764—
Reactant2-(4-Fluorophenyl)-2H-1,4-benzothiazin-3(4H)-oneHCID 13690761—
SolventTetrahydrofuranHCID 8028—
Product2-(4-fluorophenyl)-3,4-dihydro-2H-1,4-benzothiazineHCID 1898441691.2%

Reaction Steps

To a mixture of 2-(4-fluorophenyl)-3-oxo-3,4-dihydro-2H-1,4-benzothiazine (4.0 g), sodium borohydride (2.91 g) and tetrahydrofuran (100 ml) is added dropwise with stirring boron trifluoride etherate complex (12. 5 ml) at room temperature, and the mixture is refluxed for 1.5 hour. After cooling, to the mixture is added dropwise 10% hydrochloric acid (35 ml), and the mixture is further refluxed for one hour. The reaction mixture is poured into ice water and made alkaline with potassium carbonate and extracted with ethyl acetate. The ethyl acetate layer is washed, dried and distilled to remove the solvent. The residue is recrystallized from isopropyl ether to give 2-(4-fluorophenyl)-3,4-dihydro-2H-1,4-benzothiazine (3.45 g, yield 91%) as crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05246929
Source datasetuspto-grants-1993_09
ORD IDord-ac2c06d7cbfb4525b6d01a68903c4d4b
Source noteuspto-grants-1993_09